Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925804.RAYL3NUNTWMMeI39WqMK_Rl6X1tzIrOw9zsZ4XucFzWf4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925804.RAYL3NUNTWMMeI39WqMK_Rl6X1tzIrOw9zsZ4XucFzWf4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925804.RAYL3NUNTWMMeI39WqMK_Rl6X1tzIrOw9zsZ4XucFzWf4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925804.RAYL3NUNTWMMeI39WqMK_Rl6X1tzIrOw9zsZ4XucFzWf4130_provenance.
- NP925804.RAYL3NUNTWMMeI39WqMK_Rl6X1tzIrOw9zsZ4XucFzWf4130_assertion description "[The study focused on the associated brain malformations, including neuronal migration defects, which predominated in individuals with ZIC2 mutations, and neural tube defects, which were frequently associated with ZIC2 (rachischisis) and TGIF mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925804.RAYL3NUNTWMMeI39WqMK_Rl6X1tzIrOw9zsZ4XucFzWf4130_provenance.
- NP925804.RAYL3NUNTWMMeI39WqMK_Rl6X1tzIrOw9zsZ4XucFzWf4130_assertion evidence source_evidence_literature NP925804.RAYL3NUNTWMMeI39WqMK_Rl6X1tzIrOw9zsZ4XucFzWf4130_provenance.
- NP925804.RAYL3NUNTWMMeI39WqMK_Rl6X1tzIrOw9zsZ4XucFzWf4130_assertion SIO_000772 21940735 NP925804.RAYL3NUNTWMMeI39WqMK_Rl6X1tzIrOw9zsZ4XucFzWf4130_provenance.
- NP925804.RAYL3NUNTWMMeI39WqMK_Rl6X1tzIrOw9zsZ4XucFzWf4130_assertion wasDerivedFrom befree-2016 NP925804.RAYL3NUNTWMMeI39WqMK_Rl6X1tzIrOw9zsZ4XucFzWf4130_provenance.
- NP925804.RAYL3NUNTWMMeI39WqMK_Rl6X1tzIrOw9zsZ4XucFzWf4130_assertion wasGeneratedBy ECO_0000203 NP925804.RAYL3NUNTWMMeI39WqMK_Rl6X1tzIrOw9zsZ4XucFzWf4130_provenance.
- befree-2016 importedOn "2016-02-19" NP925804.RAYL3NUNTWMMeI39WqMK_Rl6X1tzIrOw9zsZ4XucFzWf4130_provenance.